EP1367093A1 - Composition de resine polyolefinique - Google Patents
Composition de resine polyolefinique Download PDFInfo
- Publication number
- EP1367093A1 EP1367093A1 EP02711323A EP02711323A EP1367093A1 EP 1367093 A1 EP1367093 A1 EP 1367093A1 EP 02711323 A EP02711323 A EP 02711323A EP 02711323 A EP02711323 A EP 02711323A EP 1367093 A1 EP1367093 A1 EP 1367093A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- polyolefin
- resin composition
- copolymer
- mol
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 0 CCC(CC)N=C* Chemical compound CCC(CC)N=C* 0.000 description 3
- OCKRQDBWYBJGDX-UHFFFAOYSA-N CCOC1CC=CCC1 Chemical compound CCOC1CC=CCC1 OCKRQDBWYBJGDX-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
- C08L23/0823—Copolymers of ethene with aliphatic cyclic olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C08L23/142—Copolymers of propene at least partially crystalline copolymers of propene with other olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/10—Peculiar tacticity
- C08L2207/12—Syndiotactic polypropylene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
Definitions
- the present invention relates to a polyolefin-based resin composition and a molded article produced therefrom. More particularly, the present invention relates to a polyolefin-based resin composition that is readily controlled in property-determining factors such as morphology and interfacial strength and is capable of providing a composite material composed of polyolefin-based resins which has properties as required, by combining optional polyolefin-based resins, especially immiscible resins, and a molded article produced from the composition.
- polyolefin-based resins have been extensively used in a variety of applications in the form of various molded articles, for example, sheets, films, injection-molded articles, blow-molded articles, foam-molded articles, vacuum-molded articles and rotational-molded articles which are formed into desired shapes or desired properties by various molding methods, because the polyolefin-based resins are chemically stable, and excellent in weather resistance, chemical resistance and mechanical strength.
- polyolefin-based resins have been noticed as resins most suitable for reducing the burden to environments because of their excellent recyclability, good moldability and formation of less harmful components upon burning. Therefore, it is expected that the polyolefin-based resins are more frequently used in future, and are required to show highly improved properties.
- Japanese Patent Application Laid-open No. Hei 2 ⁇ 281012 discloses a method of polymerizing a vinyl-based monomer or a vinylidene-based monomer using a radical polymerization initiator in the presence of a copolymer of propylene and dialkenyl benzene. Further, in Examples of the above Japanese Patent Application Laid-open No. Hei 2-281012, it is described that the thus obtained polymer is used as a miscibilizer for polypropylene and polystyrene.
- a radical polymerizable monomer is polymerized using a radical polymerization initiator to produce graft chains having an atactic structure.
- the above method fails to produce polymers having an isotactic or syndiotactic structure capable of showing a more excellent heat resistance.
- the miscibilizer is applied to a composite material composed of isotactic polypropylene and isotactic polystyrene, there is no concrete description concerning application of the miscibilizer to other composite materials.
- Japanese Patent Application Laid-open No. Hei 3-28209 discloses a graft copolymer produced by graft-polymerizing propylene to an ethylene- ⁇ -olefin-diene copolymer and a resin composition containing the graft copolymer, and further describes effects obtained by adding the graft copolymer to polypropylene and EPR.
- the graft copolymer contains gel components insoluble in a solvent, the obtained composite material is improved in properties only to a limited extent, and tends to show insufficient surface properties and poor appearance.
- the graft polymerization is usually conducted using a titanium trichloride type catalyst, the copolymerizability between diene residues and propylene is extremely low, thereby failing to achieve a high grafting rate. Therefore, since a large amount of graft sites, i.e., carbon-to-carbon unsaturated bonds remain unreacted, the obtained graft copolymer itself is inevitably deteriorated in heat stability, so that physical properties , heat stability, etc., of the composite material produced from such a graft copolymer are controlled only to a limited extent.
- the use of the above titanium trichloride type catalyst leads to not only production of polypropylene having a broad molecular weight distribution, but also production of a large amount of components soluble in ether or the like (low-stereoregular, low-molecular weight components) as well as by-products that do not contribute to improvement in miscibility, thereby causing such a problem that the obtained composite material tends to be deteriorated in physical properties.
- the object of the present invention is to provide a polyolefin-based resin composition that is readily controlled in property-determining factors such as morphology and interfacial strength and is capable of providing a composite material composed of polyolefin-based resins which has properties as required, by combining optional polyolefin-based resins, especially immiscible resins.
- the inventors have found that the above object can be achieved by a resin composition that comprises a polyolefin I, a polyolefin II having different composition and properties from those of the polyolefin I, and a specific graft copolymer, and has specific properties.
- the present invention has been accomplished on the basis of this finding.
- the present invention provides a polyolefin-based resin composition, comprising as essential components:
- the present invention provides a molded article produced from the above polyolefin-based resin composition.
- the polyolefin-based resin composition of the present invention contains as essential components, (A) a polyolefin I, (B) a polyolefin II and (C) a graft copolymer, and may also optionally contain (D) the other thermoplastic resin and/or an additive.
- the polyolefin I as the component (A) is produced from at least one monomer selected from the group consisting of C 2 to C 20 ⁇ -olefins, cyclic olefins and aromatic vinyl compounds.
- Examples of the C 2 to C 20 ⁇ -olefins include ⁇ -olefins such as ethylene, propylene, 1-butene, 3-methyl-1-butene, 4-methyl-1-butene, 4-phenyl-1-butene, 1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 3,3-dimethyl-1-pentene, 3,4-dimethyl-1-pentene, 4,4-dimethyl-1-pentene, 1-hexene, 4-methyl-1-hexene, 5-methyl-1-hexene, 6-phenyl-1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicocene and vinyl cyclohexane.
- ⁇ -olefins such as ethylene, propylene, 1-butene, 3-methyl-1-butene, 4-methyl
- halogen-substituted ⁇ -olefins such as hexafluoropropene, tetrafluoroethylene, 2-fluoropropene, fluoroethylene, 1,1-difluoroethylene, 3-fluoropropene, trifluoroethylene and 3,4-dichloro-1-butene.
- cyclic olefins examples include compounds represented by the general formula (I): wherein R 1 to R 12 are independently a hydrogen atom, a C 1 to C 20 hydrocarbon group, or a substituent group containing halogen, oxygen or nitrogen; m is an integer of 0 or larger; R 9 or R 10 and R 11 or R 12 may be bonded to each other to form a ring, and R 1 to R 12 may be the same or different.
- examples of the C 1 to C 20 hydrocarbon group as R 1 to R 12 are C 1 to C 20 alkyl groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl and hexyl; C 6 to C 20 aryl, alkylaryl or arylalkyl groups such as phenyl, tolyl and benzyl; C 1 to C 20 alkylidene groups such as methylidene, ethylidene and propylidene; or the like, with the proviso that R 1 , R 2 , R 5 and R 6 are not an alkylene group, and if any of R 3 , R 4 and R 7 to R 12 is an alkylidene group, the carbon atom to which the alkylidene group is bonded does not have any substituent group other than the alkylidene group.
- substituent group containing halogen examples include halogen atoms such as fluorine, chlorine, bromine and iodine; C 1 to C 20 halogen-substituted alkyl groups such as chloromethyl, bromomethyl and chloroethyl; or the like.
- substituent group containing oxygen examples include C 1 to C 20 alkoxy or aryloxy groups such as methoxy, ethoxy, propoxy and phenoxy; C 1 to C 20 alkoxycarbonyl groups such as methoxycarbonyl and ethoxycarbonyl; or the like.
- substituent group containing nitrogen examples include C 1 to C 20 alkylamino groups such as dimethylamino and diethylamino; cyano; or the like.
- cyclic olefins represented by the above general formula (I) include norbornene, 5-methyl norbornene, 5-ethyl norbornene, 5-propyl norbornene, 5,6-dimethyl norbornene, 1-methyl norbornene, 7-methyl norbornene, 5,5,6-trimethyl norbornene, 5-phenyl norbornene, 5-benzyl norbornene, 5-ethylidene norbornene, 1,4,5,8-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalene, 2-methyl-1,4,5,8-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalene, 2-ethyl-1,4,5,8-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalene, 2,3-dimethyl-1,4,5,8-dimethano-1,2,3,4,4a,5,8,8a-
- aromatic vinyl compounds include styrene; alkyl styrenes such as p-methyl styrene, p-ethyl styrene, p-propyl styrene, p-isopropyl styrene, p-butyl styrene, p-tert-butyl styrene, p-phenyl styrene, o-methyl styrene, o-ethyl styrene, o-propyl styrene, o-isopropyl styrene, m-methyl styrene, m-ethyl styrene, m-isopropyl styrene, m-butyl styrene, mesityl styrene, 2,4-dimethyl styrene, 2,5-d
- ethylene homopolymers and ethylene-based copolymers (1) include HDPE (high-density polyethylene), ethylene/propylene copolymer, ethylene/butene copolymer, ethylene/hexene copolymer, ethylene/octene copolymer, ethylene/decene copolymer, ethylene/eicosene copolymer, ethylene/styrene copolymer, ethylene/p-methyl styrene copolymer, ethylene/propylene/styrene tercopolymer, ethylene/p-phenyl styrene copolymer, ethylene/norbornene copolymer or the like.
- HDPE high-density polyethylene
- ethylene/propylene copolymer ethylene/butene copolymer
- ethylene/hexene copolymer ethylene/octene copolymer
- ethylene/octene copolymer
- propylene homopolymers and propylene-based copolymers (2) include isotactic polypropylene, syndiotactic polypropylene, atactic propylene, low-stereoregular isotactic polypropylene, propylene/ethylene copolymer, propylene/butene copolymer, propylene/hexene copolymer, propylene/octene copolymer, propylene/decene copolymer, propylene/eicosene copolymer, propylene/norbornene copolymer, propylene/styrene copolymer, propylene/p-methyl styrene copolymer, propylenelethylene/styrene tercopolymer, propylene/p-phenyl styrene copolymer or the like.
- C 4 to C 20 ⁇ -olefin homopolymers and C 4 to C 20 ⁇ -olefin-based copolymers (3) include polybutene, butene/ethylene copolymer, butene/propylene copolymer, butene/decene copolymer, butene/eicosene copolymer, butene/styrene copolymer, butene/ethylene/styrene tercopolymer, butene/norbornene copolymer, poly-4-methyl-penten-1, copolymers obtained by replacing butene of the above butene-based copolymers with 4-methyl-penten-1, or the like.
- aromatic vinyl compound homopolymers and aromatic vinyl compound-based copolymers (4) include isotactic polystyrene, syndiotactic polystyrene, atactic polystyrene, styrene/ethylene copolymer, styrene/propylene copolymer, styrene/ethylene/propylene tercopolymer, styrene/octene copolymer, styrene/decene copolymer, styrene/eicosene copolymer, styrene/norbornene copolymer, styrene/p-methyl styrene copolymer or the like.
- cyclic olefin homopolymers and cyclic olefin-based copolymers (5) include polynorbornene, norbornene/ethylene copolymer, norbornene/propylene copolymer, norbornene/styrene copolymer or the like.
- polyolefin I as the component (A), there may be preferably used those polyolefins having the following properties.
- the intrinsic viscosity [ ⁇ ] of the polyolefin I as measured at 135°C in decalin which is used as an index of a molecular weight thereof is preferably in the range of 0.1 to 10 deciliter/g.
- the intrinsic viscosity [ ⁇ ] is less than 1 deciliter/g, the obtained composition tends to be deteriorated in mechanical properties.
- the intrinsic viscosity [ ⁇ ] exceeds 10 deciliter/g, the obtained composition tends to be deteriorated in moldability.
- the intrinsic viscosity [ ⁇ ] of the polyolefin I is more preferably 0.15 to 8 deciliter/g, still more preferably 0.20 to 7 deciliter/g, further still more preferably 0.50 to 6 deciliter/g and most preferably 0.70 to 5 deciliter/g.
- the ratio (Mw/Mn) of weight-average molecular weight (Mw) to number-average molecular weight (Mn) thereof as measured by gel permeation chromatography (GPC) is usually in the range of 1.5 to 60.
- the steric configuration (stereoregularity) of the polyolefin I may be an isotactic, syndiotactic or atactic structure.
- the isotactic structure preferably has a pentad fraction [mmmm] of 35 to 100 mol%
- the syndiotactic structure preferably has a pentad fraction [rrrr] of 35 to 100 mol%.
- [mmmm] means a proportion of such a steric structure in which all of five side chain groups are present on the same side relative to the carbon-to-carbon bond main chain constituted by optional continuous five monomers
- [rrrr] means a proportion of such a steric structure in which five side chain groups are alternately present on the opposite sides relative to the carbon-to-carbon bond main chain constituted by optional continuous five monomers.
- the copolymerization type of the polyolefin I it may be in the form of any of a random copolymer, a block copolymer, a graft copolymer and an alternating copolymer.
- the polyolefin II as the component (B) is produced from at least one monomer selected from the group consisting of C 2 to C 20 ⁇ -olefins, cyclic olefins and aromatic vinyl compounds.
- the monomers used for production of the polyolefin II are the same as those described above for the polyolefin I.
- polyolefin II examples include the same compounds as specified above for the polyolefin I.
- the polyolefin II as the component (B) there may be used such polyolefins that are different in at least one of kinds of constituting monomer units, stereoregularity, copolymerization composition, copolymerization type and kinds of different bonds, from those of the polyolefin I.
- the condition that the polyolefins I and II are different in kinds of constituting monomer units from each other means that the polyolefins I and II is different in at least one kind of constituting monomer unit from each other, or that one of the polyolefins I and II contains such a monomer unit that is not contained in the other of the polyolefins I and II.
- this condition indicates the relationships between polyethylene and polypropylene, between ethylene/butene copolymer and polyethylene, between ethylene/butene copolymer and ethylene/octene copolymer, between propylene/butene copolymer and propylene/butene/octene tercopolymer, or the like.
- the condition that the polyolefins I and II are different in stereoregularity from each other means that the polyolefins I and II that are identical in constituting monomer units and are in the form of either homopolymers produced from the same monomer selected from the group consisting of C 3 to C 20 ⁇ -olefins, cyclic olefins and aromatic vinyl compounds, or copolymers produced from the same two or more monomers selected from the group consisting of C 2 to C 20 ⁇ -olefins, cyclic olefins and aromatic vinyl compounds, are different in stereoregularity (i.e., three steric configurations including isotactic, syndiotactic and atactic structures) from each other.
- stereoregularity i.e., three steric configurations including isotactic, syndiotactic and atactic structures
- the combination of the polyolefins I and II that are different in stereoregularity may be any of three combinations including atactic/isotactic, atactic/syndiotactic and isotactic/syndiotactic.
- the combinations of the polyolefins I and II that are different in stereoregularity from each other include isotactic polypropylene and syndiotactic polypropylene; atactic polypropylene and isotactic polypropylene; atactic polypropylene and syndiotactic polypropylene; isotactic polystyrene and syndiotactic polystyrene; atactic polystyrene and isotactic polystyrene; atactic polystyrene and syndiotactic polystyrene; low-stereoregular isotactic polypropylene and high-stereoregular isotactic polypropylene; or the like.
- the condition that the polyolefins I and II are different in copolymerization composition from each other means that the polyolefins I and II are identical in constituting monomer units, but are not identical in composition of copolymers involved.
- the monomer units constituting the copolymer are represented by a 1 , a 2 , a 3 , a 4 ⁇ a n
- the preferred combinations of the polyolefins I and II are those in which the ratio of C I (a n )/C II (a n ) or C II (a n )/C I (a n ) is preferably 1.2 or higher, more
- the polyolefins I and II are analogous in mechanical properties or thermal properties, so that the composite polyolefin-based material obtained by combining these polyolefins may fail to show improved properties as aimed by the present invention.
- the upper limit of the above ratio is not particularly restricted since the larger ratio indicates the larger difference between properties of the polyolefins I and II, so that the composition having the aimed properties can be obtained by combining these polyolefins.
- the condition that the polyolefins I and II are different in copolymerization type from each other means that the polyolefins I and II are composed of combinations of any different two copolymers selected from random copolymer, block copolymer, alternating copolymer and graft copolymer as generally defined.
- the block copolymer includes, in addition to ordinary block copolymers constituted from mutually bonded blocks each composed of monomer units with an optional length, polypropylene-based resins produced by multi-stage polymerization reaction, i.e., so-called block polypropylenes as well as stereoregular block copolymers showing such a stereoregularity which varies at every optional chain length in the molecular chain, etc.
- the condition that the polyolefins I and II are different in kinds of different bonds from each other means that the bonds contained in the polyolefins I and II are different in kind from each other.
- the different kinds of bonds include head-to-head bond and tail-to-tail bond as well as 1,3-bond in ⁇ -olefins such as propylene or styrene-based monomers.
- polyolefin II as the component (B), there may be preferably used those polyolefins having the following properties.
- the polyolefin II preferably has an intrinsic viscosity [ ⁇ ] of 0.1 to 10 deciliter/g as measured at 135°C in decalin.
- the intrinsic viscosity [ ⁇ ] of the polyolefin II is less than 0.1 deciliter/g, the obtained composition tends to be deteriorated in mechanical properties.
- the intrinsic viscosity [ ⁇ ] exceeds 10 deciliter/g, the composition tends to be deteriorated in moldability.
- the intrinsic viscosity [ ⁇ ] of the polyolefin II is more preferably 0.15 to 8 deciliter/g, still more preferably 0.20 to 7 deciliter/g, further still more preferably 0.50 to 6 deciliter/g and most preferably 0.70 to 5 deciliter/g.
- the molecular weight distribution of the polyolefin II is not particularly restricted, but is usually in such a range that the ratio (Mw/Mn) of the weight-average molecular weight (Mw) to the number-average molecular weight (Mn) thereof as measured by GPC method is 1.5 to 60.
- the graft copolymer used as the component (C) in the composition of the present invention includes those polymers obtained by bonding the above polyolefins I and II to each other through a polyene. That is, the graft copolymer contains in the same molecule, two different polyolefin-based polymers as segments which are selected from those illustrated above for the polyolefin I but are different in at least one of constituting monomer units, stereoregularity, copolymerization composition, copolymerization type and kinds of different bonds, from each other, and which are bonded to each other through a polyene,
- Segment 1 Segment 2 Combinations that are different in stereoregularity: Isotactic polypropylene Atactic polypropylene Isotactic polypropylene Syndiotactic polypropylene Atactic polypropylene Syndiotactic polypropylene Isotactic polystyrene Atactic polystyrene Isotactic polystyrene Syndiotactic polystyrene Atactic polystyrene Syndiotactic polystyrene Syndiotactic polystyrene;
- Isotactic polypropylene Ethylene/ ⁇ -olefin copolymer (propylene, butene, etc.) Isotactic polypropylene Polyethylene Syndiotactic polypropylene Polyethylene Syndiotactic polystyrene Polyethylene Isotactic polypropylene Ethylene/norbornene copolymer Isotactic polypropylene Ethylene/propylene/styrene copolymer Polyethylene Ethylene/norbornene copolymer Syndiotactic polystyrene Polyethylene Syndiotactic polystyrene Ethylene/ ⁇ -olefin copolymer (propylene, butene, etc.) Syndiotactic polystyrene Ethylene/propylene/styrene copolymer Atactic polystyrene Ethylene/propylene/styrene
- the polyene used in the graft copolymer is not particularly restricted, and may include various compounds having at least two polymerizable carbon-to-carbon double bonds in one molecule.
- the preferred polyene there may be used, for example, the following compounds (a) to (e):
- Examples of the ⁇ , ⁇ -type polyenes include 1,3-butadiene, 1,4-pentadiene, 1,5-hexadiene, 1,6-heptadiene, 1,7-octadiene, 1,8-nonadiene, 1,9-decadiene, 1,10-undecadiene, 1,11-dodecadiene, 1,13-tetradecadiene, 1,15-hexadecadiene, 4-methyl-1,9-decadiene, 4,4-dimethyl-1,9-decadiene, 5-allyl-1,9-decadiene, 1,19-eicodiene or the like.
- R 13 is a hydrogen atom, a halogen atom or a substituent group containing carbon and/or silicon;
- R 14 is a substituent group containing an ⁇ -olefin residue; and
- a is an integer of 1 to 4 with the proviso that when a is 2 or larger, the plural R 13 groups may be the same or different.
- styrene-type polyenes examples include p-divinylbenzene, m-divinylbenzene, o-divinylbenzene, di(p-vinylphenyl)methane, 1,3-bis(p-vinylphenyl)propane, 1,5-bis(p-vinylphenyl)pentane or the like.
- Examples of the halogen atom as R 15 to R 24 include chlorine, fluorine, bromine, etc.
- Examples of the C 1 to C 20 hydrocarbon group as R 15 to R 24 include methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclohexyl, octyl, decyl, dodecyl, tetradecyl, pentadecyl, heptadecyl, octadecyl, etc., as well as corresponding alkoxy groups thereof.
- the R 15 to R 24 groups may be the same or different.
- Specific examples of the compounds represented by the above general formula (IV) include 5-vinyl-2-norbornene, 5-(3-butenyl)-2-norbornene, 5-allyl-2-norbornene, 5-(4-pentenyl)-2-norbornene, 5-(7-octenyl)-2-norbornene or the like.
- Specific examples of the compounds represented by the above general formula (V) include cyclopentadiene, dimethyl dicyclopentadiene, diethyl dicyclopentadiene or the like.
- cyclic polyenes (c) there may be used compounds represented by the general formula (VI): wherein b is 0, 1 or 2.
- Examples of the compounds represented by the general formula (VI) include bicyclo[2.2.1.]hepto-2,5-diene, tetracyclo[4.4.0.1 2,5 .1 7,10 ]-3,8-dodecadiene,hexacyclo[6.6.1.1 3,6 .1 10,13 .0 2,7 .0 9,1 4]-4,11-heptadecadiene or the like.
- cyclic polyenes (c) there may also be used compounds represented by the general formula (VII): wherein c is an integer of 1 or 2; and d is an integer of 0 to 11, and compounds represented by the general formula (VIII): wherein e is an integer of 0 to 6.
- Examples of the compounds represented by the general formula (VII) include 5-vinyl bicyclo[2.2.1]hepto-2-ene, 5-allyl bicyclo[2.2.1]hepto-2-ene, 5-(3-butenyl)bicyclo[2.2.1]hepto-2-ene, 8-vinyl tetracyclo[4.4.0.1 2,5 .1 7,10 ]-3-dodecene, 11-vinyl hexacyclo[6.6.1.1 3,6 .1 10,13 .0 2,7 .0 9,14 ]-4-heptadecene or the like.
- Examples of the compounds represented by the general formula (VIII) include 1,1-bis(5-bicyclo[2.2.1]hept-2-enyl)methane, 1,2-bis(5-bicyclo[2.2.1]hept-2-enyl) ethane, 1,6-bis(5-bicyclo[2.2.1]hept-2-enyl)hexane or the like.
- R 25 is a divalent C 1 to C 20 hydrocarbon group
- R 26 is a halogen atom or a C 1 to C 8 hydrocarbon group
- R 27 and R 28 are independently a hydrogen atom, a halogen atom or a C 1 to C 8 hydrocarbon group
- f is an integer of 0 to 4.
- Examples of the divalent C 1 to C 20 hydrocarbon group as R 25 in the general formula (IX) include C 1 to C 20 alkylene, C 6 to C 20 arylene, C 7 to C 20 alkylarylene, C 7 to C 20 arylalkylene or the like.
- Specific examples of the divalent C 1 to C 20 hydrocarbon group as R 25 include methylene, ethylene, propylene, butylene, pentylene, hexylene, phenylene, tolylene or the like.
- Examples of the halogen atom as R 26 include chlorine, bromine, fluorine and iodine.
- Examples of the C 1 to C 8 hydrocarbon group as R 26 include saturated hydrocarbon groups, typically, for example, alkyl groups such as methyl, ethyl, propyl, butyl and pentyl, unsaturated hydrocarbon groups such as vinyl, or the like.
- Examples of the halogen atom and the C 1 to C 8 hydrocarbon group as R 27 and R 28 are the same as described above.
- R 25 is alkylene
- examples of the compounds represented by the general formula (IX) in which R 25 is alkylene include p-(2-propenyl)styrene, m-(2-propenyl)styrene, p-(3-butenyl)styrene, m-(3-butenyl)styrene, o-(3-butenyl)styrene, p-(4-pentenyl)styrene, m-(4-pentenyl)styrene, o-(4-pentenyl)styrene, p-(7-octenyl)styrene, p-(1-methyl-3-butenyl)styrene, p-(2-methyl-3-butenyl)styrene, m-(2-methyl-3-butenyl)styrene, o-(2-methyl-3-butenyl)s
- R 25 is arylene
- specific examples of the compounds represented by the general formula (IX) in which R 25 is arylene include 4-vinyl-4'-(3-butenyl)biphenyl, 4-vinyl-3'-(3-butenyl)biphenyl, 4-vinyl-4'-(4-pentenyl)biphenyl, 4-vinyl-2'-(4-pentenyl)biphenyl, 4-vinyl-4'-(2-methyl-3-butenyl)biphenyl or the like.
- monoalicyclic diene compounds there may be used monoalicyclic diene compounds.
- the monoalicyclic diene compounds include 1,4-cyclohexadiene, 1,5-cyclooctadiene, 1,5-cyclododecadiene, 4-vinyl cyclohexane, 1-allyl-4-isopropylidene cyclohexane, 3-allyl cyclopentene, 4-allyl cyclohexene, 1-isopropenyl-4-(4-butenyl)cyclohexane or the like.
- polyenes preferred are those polyenes having a high-polymerizable carbon-to-carbon bonds and containing a less amount of residual unsaturated bonds that tend to cause deterioration in thermal stability upon production of the composition.
- preferred polyenes are the ⁇ -, ⁇ -type polyenes (a), the styrene-type polyenes (b), the compounds (c) represented by the general formulae (VI), (VII) and (VIII), and the styrene/ ⁇ -olefin-type polyenes (d).
- the graft copolymer as the component (C) is required to have a 140°C xylene insoluble content of 0 to 2.5% by weight.
- the graft copolymer is insufficiently dispersed and mixed in a melt or solution upon production of the resin composition, thereby failing to obtain the composition having the aimed properties, and further a molded article produced therefrom tends to show a poor appearance and suffer from deterioration in breaking strength due to concentrated stress.
- the 140°C xylene insoluble content of the graft copolymer (C) is preferably 0 to 1.5% by weight, more preferably 0 to 1.2% by weight, still more preferably 0 to 1.0% by weight, further still more preferably 0 to 0.5% by weight and most preferably 0 to 0.3% by weight.
- the above xylene insoluble content is measured by the following method. That is, 2.0 g of the graft copolymer is placed in a 150 mesh stainless steel container, immersed in one liter of p-xylene at 140°C and dissolved therein while stirring for 5 hours. After completion of the dissolution, the container is removed from the p-xylene bath, and the residual graft copolymer in the container is dried at 100°C under reduced pressure until reaching a constant weight. The weight of the graft copolymer remaining in the container is divided by the weight of the graft copolymer initially charged to determine the p-xylene insoluble content (%) in the graft copolymer.
- the graft copolymer as the component (C) may be generally produced by the following method, i.e., the method comprising the step [step 1] of producing an polyolefin containing a polyene residue, and the step [step 2] of subjecting the polyolefin obtained in the step 1 to graft copolymerization.
- the following methods can be adopted.
- the method (i) it is preferred to use a slurry polymerization process for the step 1, arid use a washing solvent incapable of dissolving the obtained polyolefin containing a polyene residue, since the polyolefin resin composition of the present invention can be produced with a high efficiency.
- the graft copolymer as the component (C) contains a polyene unit as an essential unit.
- the polyene unit content [D] in the graft copolymer is as small as usually 0.45 mol% or lower, preferably 0.40 mol% or lower, more preferably 0.35 mol% or lower, still more preferably 0.30 mol% or lower, further still more preferably 0.25 mol% or lower and most preferably 0.20 mol% or lower.
- the polyene unit content [D] exceeds 0.45 mol%, there tends to arise the same problem as in the case where the xylene insoluble content exceeds 2.5% by weight.
- the polyene unit content [D] may be measured by the following method.
- the graft copolymer contains a small polyene unit content, it is required to select a measuring method suitable for detecting even a trace amount of the polyene unit.
- the shear rate dependency of melt viscosity of the polyolefin having such a branched structure due to the polyene unit is larger than that of the polyolefin containing no branched structure. Therefore, the polyene unit forming the branched structure can be detected by comparing the shear rate dependency of melt viscosity of the graft copolymer with that of the polymer produced under the same conditions as those of the graft copolymer except for using no polyene.
- the above method is adversely affected by the molecular weight distribution of the polymer to be measured.
- the shear rate dependency of melt viscosity of the graft copolymer relative to its molecular weight distribution with that of the polyolefin apparently having no branched structure and containing the same kind of constituting monomer unit at the substantially same content, the polyene unit forming the branched structure can be surely detected.
- a polyolefin which is produced under the same conditions as those of the graft copolymer except for using no polyene, and has a molecular weight distribution [weight-average molecular weight (Mw)/number-average molecular weight (Mn)] of 0.8 to 1.8 times that of the graft copolymer:
- the polyene unit content in the graft copolymer is determined by the following method.
- the "same content of constituting monomer units" means that the comparative specimen is made of either one of the following materials:
- the molecular weight distribution (Mw/Mn) and N 1 of the graft copolymer are measured, and the values N 0 and N 1 are compared with each other under the same molecular weight distribution.
- the existence of the polyene unit in the graft copolymer can be confirmed when the ratio of N 1 /N 0 satisfies the following formula (a): 1.05 ⁇ N 1 /N 0 ⁇ 80 preferably 1.10 ⁇ N 1 /N 0 ⁇ 80 more preferably 1.30 ⁇ N 1 /N 0 ⁇ 70 still more preferably 1.50 ⁇ N 1 /N 0 ⁇ 65 further still more preferably 1.70 ⁇ N 1 /N 0 ⁇ 60 most preferably 2.00 ⁇ N 1 /N 0 ⁇ 55
- the ratio N 1 /N 0 is less than 1.05, the graft copolymer tends to be deteriorated in miscibility, thereby failing to obtain a composite material exhibiting sufficient physical properties.
- the ratio N 1 /N 0 exceeds 80, graft copolymers having a cross-linked structure are by-produced, resulting in formation of gels and, therefore, poor mixing property upon production of the composite material.
- the graft copolymer as the component (C) is required to contain residual carbon-to-carbon double bonds derived from the polyene unit in an amount of 0 to 0.15 mol%.
- the residual unsaturated bonds defined herein mean those derived from the polyene unit, but do not involve carbon-to-carbon double bonds bonded to terminals of polymers newly produced during the production process.
- the amount of the residual carbon-to-carbon double bonds exceeds 0.15 mol%, the obtained composition tends to be deteriorated in weather resistance and thermal stability.
- the amount of the residual carbon-to-carbon double bonds contained in the graft copolymer is preferably 0 to 0.13 mol%, more preferably 0 to 0.11 mol%, still more preferably 0 to 0.09 mol%, further still more preferably 0 to 0.07 mol% and most preferably 0 to 0.05 mol%.
- the amount of the residual carbon-to-carbon double bonds is usually 0 to 30 mol%, preferably 0 to 28 mol%, more preferably 0 to 25 mol%, still more preferably 0 to 22 mol%, further still more preferably 0 to 18 mol% and most preferably 0 to 15 mol% based on the polyene unit.
- the amount of the residual carbon-to-carbon double bonds derived from the polyene unit can be measured according to ordinary methods such as infrared absorption spectrum method and ultraviolet absorption spectrum method. Since the graft copolymer inherently contains a very small amount of the polyene unit, the amount of the unreacted carbon-to-carbon double bonds is further reduced. Therefore, if the amount of the residual carbon-to-carbon double bonds is below the detection limits of the above measuring methods and is therefore unmeasurable, the graft copolymer is regarded to contain substantially no unreacted carbon-to-carbon double bonds therein.
- the graft copolymer as the component (C) may be generally produced by the following method, i.e., the method comprising the step [step 1] of producing a polyolefin containing a polyene residue, and the step [step 2] of subjecting the polyolefin obtained in the step 1 to graft copolymerization.
- the following methods can be adopted.
- a catalyst there may be used catalysts employed in the below-mentioned Production Examples.
- the graft copolymer as the component (C) is a graft copolymer containing segments having substantially the same chain structures as those of the polyolefin I as the component (A) and the polyolefin II as the component (B), respectively, which are bonded to each other through a polyene, in the same molecule.
- the graft copolymer (C) is not particularly limited in its structure as long as it exhibits a xylene insoluble content and an amount of unreacted carbon-to-carbon unsaturated bonds as defined in the present invention, and satisfies the condition that a relaxation velocity ratio of the resultant composition as measured by solid 1 H-NMR method lies in the range as defined in the present invention.
- the graft copolymer has the following intrinsic viscosity, stereoregularity and copolymerization composition.
- the intrinsic viscosity [ ⁇ ] of the graft copolymer (C) as measured at 135°C in decalin is preferably 0.1 to 10 deciliter/g, more preferably 0.2 to 9 deciliter/g, still more preferably 0.3 to 8 deciliter/g and most preferably 0.4 to 7 deciliter/g.
- the intrinsic viscosity [ ⁇ ] is less than 0.1 deciliter/g, it may be difficult to well control properties of the obtained composition.
- the intrinsic viscosity [ ⁇ ] exceeds 10 deciliter/g, the graft copolymer tends to be deteriorated in dispersibility upon production of the composition.
- the ratio of (mmmm)g/(mmmm)po or the ratio of (rrrr)g/(rrrr)po is preferably 0.5 to 1.5, more preferably 0.6 to 1.4, still more preferably 0.65 to 1.35, further still more preferably 0.67 to 1.30 and most preferably 0.70 to 1.25.
- the (mmmm)g or (rrrr)g represents the stereoregularity of the graft copolymer
- the (mmmm)po or (rrrr)po represents the stereoregularity of a portion of the polyolefin I or polyolefin II corresponding to the respective segments of the graft copolymer.
- the ratio is less than 0.5 or exceeds 1.5, the graft copolymer tends to be deteriorated in miscibility with the polyolefin I or polyolefin II, thereby failing to improve properties of the obtained composition.
- compositions of respective monomer units present in the polyolefin I or II are represented by a po , b po , C po ⁇ , n po .
- compositions of respective monomer units present in the segments of the graft copolymer corresponding to polyolefin I or II are represented by a g , bg, C g ⁇ , n g .
- the maximum value of the ratio of n po /n g or n g /n po is preferably 20 or smaller, and the minimum value of the ratio is preferably 1.5 or smaller.
- the ratio is out of the above-specified range, the obtained composite material tends to be insufficient in physical properties thereof.
- the ratio is within the above range, there occurs no problem even though a small amount of the third monomer unit is contained in the graft copolymer.
- the content of the third monomer unit in the graft copolymer is usually 3 mol% or smaller.
- the greater value of the ratio of n po /n g or n g /n po is more preferably 15 or smaller, still more preferably 10 or smaller, further still more preferably 8 or smaller and most preferably 5 or smaller, and the little value of the ratio of n po /n g or n g /n po is more preferably 1.4 or smaller, still more preferably 1.3 or smaller, further still more preferably 1.25 or smaller and most preferably 1.20 or smaller.
- the graft copolymer as the component (C) may be produced, for example, by slurry polymerization, solution polymerization, gas phase polymerization, bulk polymerization, etc., using a metallocene-based catalyst as a main catalyst together with a co-catalyst composed of chain or cyclic aluminoxane, an ionic compound such as tetrakis(pentafluorophenyl)boric acid N,N-dimethyl anilinium, or a Lewis acid such as triphenyl boric acid.
- This production method generally comprises the step [step 1] of producing a polyolefin containing a polyene residue, and the step [step 2] of subjecting the polyolefin obtained in the step 1 to graft copolymerization.
- the polyolefin-based resin composition of the present invention may contain, in addition to the polyolefin I as the component (A), the polyolefin II as the component (B) and the graft copolymer as the component (C), the other thermoplastic resin as the component (D) and/or an additive, if desired.
- the suitable combination of the components of the polyolefin-based resin composition according to the present invention include polyolefin I/polyolefin II/graft copolymer, polyolefin I/polyolefin II/graft copolymer/thermoplastic resin, polyolefin I/polyolefin II/graft copolymer/additive, and polyolefin I/polyolefin II/graft copolymer/thermoplastic resin/additive.
- the polyolefin I as the component (A) and the polyolefin II as the component (B) are preferably used in a weight ratio of 1:99 to 99:1.
- the graft copolymer as the component (C) is preferably used in an amount of 0.01 to 30% by weight, more preferably 0.05 to 28% by weight, still more preferably 0.10 to 26% by weight, further still more preferably 0.20 to 24% by weight and most preferably 0.50 to 22% by weight based on the total weight of the components (A) and (B).
- the amount of the component (C) used is less than 0.01% by weight or exceeds 30% by weight, the obtained composition tends to fail to exhibit aimed properties.
- thermoplastic resin as the component (D) is added in an amount of usually 0.5 to 60% by weight based on the total weight of the components (A), (B) and (C), and the additive is added in an amount of usually 0.0001 to 60% by weight based on the total weight of the components (A), (B) and (C).
- the polyolefin-based resin composition of the present invention has a relaxation velocity (1/R 1 ) of its long-term relaxation component of preferably 0.2 to 10 (1/sec), more preferably 0.3 to 9 (1/sec) and still more preferably 0.35 to 5 (1/sec) as measured by solid 1 H-NMR method.
- the composition of the present invention is required to satisfy the condition that a ratio [(1/R 1 )/(1/R 1 ) 0 ] of the relaxation velocity (1/R 1 ) of the long-term relaxation component measured by solid 1 H-NMR method about the composition to a relaxation velocity (1/R 1 ) 0 of a long-term relaxation component measured by solid 1 H-NMR method about a resin mixture composed of only the components (A) and (B) is 1.01 or higher.
- the ratio [(1/R 1 )/(1/R 1 ) 0 ] is less than 1.01, the resins tends to be deteriorated in miscibility with each other, thereby failing to obtain the composition having the aimed properties.
- the ratio [(1/R 1 )/(1/R 1 ) 0 ] is preferably 1.02 or higher and more preferably 1.03 or higher.
- the ratio [(1/R 1 )/(1/R 1 ) 0 ] is measured by an inverted restoration method (180°- ⁇ -90° pulse method) using the following solid 1 H-NMR measuring device.
- Apparatus "CPX-902" produced by Bluker Inc.
- Nucleus to be measured Hydrogen nucleus ( 1 H)
- Measuring frequency 90 MHz
- Measuring temperature The relaxation velocities of the long-term relaxation components of the polyolefins I and II can be optionally set in different temperature ranges.
- the relaxation velocities of the long-term relaxation components of the polyolefins I and II are measured in a temperature of from 0°C to 150°C, preferably in such a temperature range in which the difference therebetween becomes largest.
- 90° pulse width 2.4 to 2.5 microseconds
- the relaxation velocity ratio [(1/R 1 )/(1/R 1 ) 0 ] can be adjusted to 1.01 or higher, for example, by adopting the following methods for controlling the graft copolymer contained in the polyolefin-based resin composition.
- the composition of thee present invention is required to have an intrinsic viscosity [ ⁇ ] of 0.1 to 10 deciliter/g as measured at 135°C in decalin.
- the intrinsic viscosity [ ⁇ ] of the composition is less than 0.1 deciliter/g, the composition tends to be insufficient in mechanical properties.
- the intrinsic viscosity [ ⁇ ] of the composition exceeds 10 deciliter/g, the composition tends to be deteriorated in moldability.
- the intrinsic viscosity [ ⁇ ] of the composition is preferably 0.15 to 8 deciliter/g, more preferably 0.20 to 7 deciliter/g, still more preferably 0.50 to 6 deciliter/g and most preferably 0.70 to 5 deciliter/g.
- polyolefin I as the component (A) and the polyolefin II as the component (B) used in the polyolefin-based resin composition of the present invention
- one of the polyolefins I and II is first selected to clearly determine physical properties and functions to be improved as well as properties to be further added thereto. Then, the other polyolefin having the physical properties and functions to be improved as well as the properties to be further added is selected.
- Examples of the physical properties and functions to be improved as well as the properties to be further added include transparency, elastic modulus, heat resistance, yield strength, breaking strength, low-temperature impact strength, heat sealing temperature, strength, tear strength, breaking elongation, crystallizability, melting point, solvent resistance, surface hardness, surface glossiness, shrinkage rate upon molding, appearance such as flow marks, mold-shape transferring property, etc.
- the polyolefins may be selected, for example, in view of their properties that can be controlled by stereoregularity or by varying the copolymerization composition or kinds of constituting monomers.
- Examples of the properties of the polyolefins which can be controlled by stereoregularity are heat resistance, elastic modulus, strength, crystallizability, melting point, solvent resistance, shrinkage rate upon molding, impact strength, etc.
- Examples of the properties of the polyolefins which can be controlled by varying the copolymerization composition are transparency, elastic modulus, heat resistance, tensile strength, breaking strength, low-temperature impact strength, heat sealing temperature, strength, tear strength, breaking elongation, etc.
- Examples of the properties of the polyolefins which can be controlled by varying the kinds of constituting monomers include all of the above-described properties since the properties of the polyolefins are most remarkably influenced by the kinds of constituting monomers, thereby realizing a broad range of properties by combining the suitable monomers.
- thermoplastic resin as the component (D) which may be optionally blended in the polyolefin-based resin composition of the present invention, include (1) polyolefins exemplified above for the polyolefins I and II except for the polyolefins used as the constituting components of the composition; (2) copolymers of olefin and a vinyl monomer, more specifically, ethylene/vinyl acetate copolymer, ethylene/acrylic acid copolymer, ethylene/ethyl acrylate copolymer, ethylene/methyl methacrylate copolymer, ionomers (metal ion-substituted products of ethylene/carboxylic acid-containing monomer copolymers such as sodium ion-neutralized products of ethylene/acrylic acid copolymer), ethylene/vinyl alcohol copolymer or the like; (3) modified olefin copolymers, more specifically, maleic anhydride-modified polypropylene, male
- additives examples include nucleating agents, antioxidants, hydrochloric acid absorbers, heat stabilizers, light stabilizers, ultraviolet radiation absorbents, lubricants, antistatic agents, flame retardants, pigments, dyes, dispersants, copper inhibitors, neutralizers, foaming agents, plasticizers, defoamers, cross-linking agents, flow modifiers such as peroxides, weld strength modifiers or the like.
- antioxidants there may be used phenol-based, sulfur-based and phosphorus-based antioxidants, etc.
- phenol-based antioxidants include phenols such as 2,6-di-tert-butyl-p-cresol, stearyl (3,3-dimethyl-4-hydroxybenzyl)thioglycolate, stearyl- ⁇ -(4-hydroxy-3,5-di-tert-butylphenol)propionate, distearyl-3,5-di-tert-butyl-4-hydroxybenzyl phosphonate, 2,4,6-tris(3',5'-di-tert-butyl-4'-hydroxybenzylthio)-1,3,5-triazine, distearyl (4-hydroxy-3-methyl-5-tert-butylbenzyl)malonate, 2,2'-methylenebis(4-methyl-6-tert-butylphenol), 4,4'-methylenebis(2,6-di-tert-butylphenol),
- sulfur-based antioxidants examples include dialkylthiodipropionates such as dilaurylthiodipropionate, dimyristylthiodipropionate and distearylthiodipropionate; esters of an alkylthiopropionic acid such as butylthiopropionic acid, octylthiopropionic acid, laurylthiopropionic acid and stearylthiopropionic acid, and a polyhydric alcohol such as glycerol, trimethylol ethane, trimethylol propane, pentaerythritol and trishydroxyethyl isocyanurate, for example, pentaerythritol tetralaurylthiopropionate; or the like.
- dialkylthiodipropionates such as dilaurylthiodipropionate, dimyristylthiodipropionate and distearylthiodipropionate
- Examples of the phosphorus-based antioxidants include trioctyl phosphite, tirlauryl phosphite, tridecyl phosphite, octyl diphenyl phosphite, tris(2,4-di-tert-butylphenyl)phosphite, triphenyl phosphite, tris(butoxyethyl)phosphite, tris(nonylphenyl) phosphite, distearyl pentaerythritol diphosphite, tetra(tridecyl)-1,1,3-tris(2-methyl-5-tert-butyl-4-hydroxyphenyl)butane diphosphite, tetra-(C 12 to C 15 mixed alkyl)-4,4'-isopropylidenediphenyl diphosphite, tetra(tridecyl)-4,4'-butyliden
- 6-hydroxy chroman derivatives for example, various tocopherols such as ⁇ - , ⁇ - , ⁇ - and ⁇ -tocopherols and mixtures thereof, 2,5-dimethyl-, 2,5,8-trimethyl-and 2,5,7,8-tetramethyl-substituted products of 2-(4-methyl-pent-3-enyl)-6-hydroxy chroman, 2,2,7-trimethyl-5-tert-butyl-6-hydroxy chroman, 2,2,5-trimethyl-7-tert-butyl-6-hydroxy chroman, 2,2,5-trimethyl-6-tert-butyl-6-hydroxy chroman, 2,2-dimethyl-5-tert-butyl-6-hydroxy chroman or the like.
- various tocopherols such as ⁇ - , ⁇ - , ⁇ - and ⁇ -tocopherols and mixtures thereof, 2,5-dimethyl-, 2,5,8-trimethyl-and 2,5,7,8-tetra
- the antioxidant may be usually used in an amount of 0.0001 to 10% by weight based on the total weight of the composition.
- hydrochloric acid absorbers examples include composite compounds such as Mg 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O, Mg 8 Al 2 (OH) 20 CO 3 ⁇ 5H 2 O, Mg 5 Al 2 (OH) 14 CO 3 ⁇ 4H 2 O, Mg 10 Al 2 (OH) 22 (CO 3 ) 2 ⁇ 4H 2 O, Mg 6 Al 2 (OH) 16 HPO 4 ⁇ 4H 2 O, Ca 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O, Zn 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O, Zn 6 Al 2 (OH) 16 SO 4 ⁇ 4H 2 O, Mg 6 Al 2 (OH) 16 SO 4 ⁇ 4H 2 O and Mg 6 Al 2 (OH) 12 CO 3 ⁇ 3H 2 O, calcium stearate, etc.
- composite compounds such as Mg 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O, Mg 8 Al 2 (OH) 20 CO 3 ⁇ 5H 2 O, Mg 5 Al 2 (OH
- ultraviolet radiation absorbents and the light stabilizers examples include hydroxybenzophenones such as 2-hydroxy-4-methoxy benzophenone, 2-hydroxy-4-n-octoxy benzophenone, 2,2'-dihydroxy-4-methoxy benzophenone and 2,4-dihydroxybenzophenone; benzotriazoles such as 2-(2'-hydroxy-3'-tert-butyl-5'-methylphenyl)-5-chlorobenzotriazole, 2-(2'-hydroxy-3',5'-di-tert-butylphenyl)-5-chlorobenzotriazole, 2-(2'-hydroxy-5'-methylphenyl) benzotriazole and 2-(2'-hydroxy-3',5'-di-tert-amylphenyl) benzotriazole; benzoates such as phenyl salicylate, p-tert-butylphenyl salicylate, 2,4-di-tert-butylphenyl-3,5-
- These ultraviolet radiation absorbents and light stabilizers may be usually added in an amount of 0.0001 to 10% by weight based on the total weight of the composition.
- lubricants examples include aliphatic hydrocarbons such as paraffin waxes, polyethylene waxes and polypropylene waxes; higher fatty acids such as capric acid, lauric acid, myristic acid, palmitic acid, margaric acid, stearic acid, arachidic acid and behenic acid or metal salts thereof such as lithium salts, calcium salts, sodium salts, magnesium salts and potassium salts; aliphatic alcohols such as palmityl alcohol, cetyl alcohol and stearyl alcohol; aliphatic amides such as caproamide, caprylamide, caprinamide, laurylamide, myristylamide, palmitylamide and stearamide; esters of fatty acids and alcohols; fluorine compounds such as fluoroalkyl carboxylic acids or metal salts thereof and fluoroalkyl sulfonic acid metal salts, or the like.
- aliphatic hydrocarbons such as paraffin waxes, polyethylene waxes and polypropylene wax
- the nucleating agents used in the present invention may be appropriately optionally selected from conventional known nucleating agents.
- the suitable nucleating agents are aromatic phosphoric acid ester salts or dibenzylidene sorbitol.
- aromatic phosphoric acid ester salts there may be used, for example, compounds represented by the general formula (X): wherein R 29 is an oxygen atom, a sulfur atom or a C 1 to C 10 divalent hydrocarbon group; R 30 and R 31 are independently a hydrogen atom or a C 1 to C 10 hydrocarbon group in which R 30 and R 31 may be the same or different, and the two R 30 groups, the two R 31 groups or R 30 and R 31 may be respectively bonded to each other to from a ring; M is a mono- to tri-valent metal atom; and g is an integer of 1 to 3, and compounds represented by the general formula (XI): wherein R 32 is a hydrogen atom or a C 1 to C 10 hydrocarbon group; and M and g are the same as defined above.
- Examples of the compounds represented by the general formula (X) include sodium-2,2'-methylene-bis(4,6-di-tert-butylphenyl)phosphate, sodium-2,2'-ethylidene-bis(4,6-di-tert-butylphenyl)phosphate, lithium-2,2'-methylene-bis(4,6-di-tert-butylphenyl)phosphate, lithium-2,2'-ethylidene-bis(4,6-di-tert-butylphenyl)phosphate, sodium-2,2'-ethylidene-bis(4-isopropyl-6-tert-butylphenyl)phosphate, lithium-2,2'-methylene-bis(4-methyl-6-tert-butylphenyl)phosphate, lithium-2,2'-methylene-bis(4-ethyl-6-tert-butylphenyl)phosphate, calcium-bis[2,2'-thiobis(4-methyl
- Examples of the compounds represented by the general formula (XI) include sodium-bis(4-tert-butylphenyl)phosphate, sodium-bis(4-methylphenyl)phosphate, sodium-bis(4-ethylphenyl)phosphate, sodium-bis(4-isopropylphenyl)phosphate, sodium-bis(4-tert-octylphenyl)phosphate, potassium-bis(4-tert-butylphenyl)phosphate, calcium-bis(4-tert-butylphenyl)phosphate, magnesium-bis(4-tert-butylphenyl)phosphate, lithium-bis(4-tert-butylphenyl)phosphate, aluminum-bis(4-tert-butylphenyl)phosphate and combinations thereof. Of these compounds, preferred is sodium-bis(4-tert-butylphenyl)phosphate.
- dibenzylidene sorbitol there may be used, for example, compounds represented by the general formula (XII): wherein R 33 is a hydrogen atom or a C 1 to C 10 hydrocarbon group.
- Examples of the compounds represented by the general formula (XII) include 1,3,2,4-dibenzylidene sorbitol, 1,3-benzylidene-2,4-p-methyl benzylidene sorbitol, 1,3-benzylidene-2,4-p-ethyl benzylidene sorbitol, 1,3-p-methylbenzylidene-2,4-benzylidene sorbitol, 1,3-p-ethylbenzylidene-2,4-benzylidene sorbitol, 1,3-p-methylbenzylidene-2,4-p-ethylbenzylidene sorbitol, 1,3-p-ethylbenzylidene-2,4-p-methylbenzylidene sorbitol, 1,3,2,4-di(p-methylbenzylidene) sorbitol, 1,3,2, 4-di(p-ethylbenzylidene) sorbi
- 1,3,2,4-dibenzylidene sorbitol 1,3,2,4-di(p-methylbenzylidene) sorbitol, 1,3,2,4-di(p-ethylbenzylidene) sorbitol, 1,3-p-chlorobenzylidene-2,4-p-methylbenzylidene sorbitol, 1,3,2,4-di(p-chlorobenzylidene) sorbitol and combinations thereof.
- nucleating agents there may also be used metal salts of aromatic carboxylic acids, metal salts of aliphatic carboxylic acids or the like.
- metal salts include aluminum benzoate, aluminum p-tert-butyl benzoate, sodium adipate, sodium thiophenecarboxylate, sodium pyrrolecarboxylate or the like.
- polymers such as poly-4-methyl penten-1, and inorganic compounds such as talc.
- the nucleating agent may be usually added in an amount of 0.0001 to 10% by weight based on the total weight of the composition.
- the composition of the present invention may further contain inorganic fillers.
- the inorganic fillers usable in the present invention include powered fillers, e.g., natural silicic acid or silicates such as fine talc powder, kaolinite, calcined clay, pyrophyllite, sericite and wollastonite, carbonates such as precipitated calcium carbonate, heavy calcium carbonate and magnesium carbonate, hydroxides such as aluminum hydroxide and magnesium hydroxide, oxides such as zinc oxide, zinc white and magnesium oxide, and synthetic silicic acid or silicates such as hydrous calcium silicate, hydrous aluminum silicate, hydrous silicic acid and anhydrous silicic acid; flake-like fillers such as mica; fibrous fillers such as basic magnesium sulfate whiskers, calcium titanate whiskers, aluminum borate whiskers, sepiolite, PMF (processed mineral fibers), xonotlite, potassium titanate and ellestadite; balloon-shaped fillers such as glass balloons and fly ash
- the polyolefin-based resin composition of the present invention can be produced by conventionally known methods without any particular limitation, such as the melt-kneading method using a kneader or extruder, and the method of dissolving or dispersing the constituting components in a solvent, and then removing the solvent from the resultant solution or pouring the solution into a poor solvent for the polymer to obtain the composition.
- the polyolefin-based resin composition can be produced by first kneading the components using a kneading apparatus such as a single-screw extruder, a twin-screw extruder, a twin-screw kneader, a Babury mixer and rolls, and then forming the kneaded material into usually pellets.
- a kneading apparatus such as a single-screw extruder, a twin-screw extruder, a twin-screw kneader, a Babury mixer and rolls, and then forming the kneaded material into usually pellets.
- the molded article of the present invention is formed by molding the thus obtained polyolefin-based resin composition by (1) method of forming the composition into a two-dimensional shape through a die, or (2) method of forming the composition into a three-dimensional shape using a metal mold or die.
- the molding method (1) include extrusion molding, profile molding, spinning, non-woven fabric molding, multi-layer molding, etc.
- Examples of the molding method (2) include injection molding, blow molding, vacuum molding, etc.
- molded article of the present invention include films, sheets, pipes, hollow molded products, fibers, injection-molded products, fabricated sheets, non-woven fabrics, multi-layer sheets or the like.
- the solution separated from the precipitate was filtered through a G5 glass filter to obtain toluene-soluble methyl aluminoxane.
- concentration of the toluene-soluble methyl aluminoxane was 1.06 mol/liter.
- the obtained reaction mixture was held at 60°C, and the solid component thereof was washed with 200 milliliter of dehydrated toluene twice and then with 200 milliliter of dehydrated heptane twice.
- the obtained solids were dried at 50°C under reduced pressure to obtain 32.8 g of SiO 2 -supported methyl aluminoxane.
- the thus obtained SiO 2 -supported methyl aluminoxane was charged again into dehydrated heptane and preserved in the form of a slurry.
- a 50 milliliter Schlenk tube was dried and purged with nitrogen, and then charged with 10 milliliter of dried heptane and 2 millimol (in terms of aluminum atom) of the SiO 2 -supported methyl aluminoxane prepared in the above step (2), followed by stirring.
- the resultant mixture was prepolymerized at 25°C under an ethylene pressure of 0.2 MPa for 30 minutes to activate the catalyst, and then subjected to depressurization and blowing with nitrogen to remove unreacted ethylene therefrom. Then, 0.81 milliliter of a heptane solution containing 0.5 millimol of 1,9-decadiene was added to the obtained reaction solution, and then hydrogen was introduced thereinto until reaching 0.02 MPa. After setting the reaction temperature at 60°C and introducing ethylene until reaching an ethylene partial pressure of 0.7 MPa, the polymerization reaction was initiated and continued for 210 minutes while controlling the reaction temperature to obtain polyethylene.
- the resultant reaction solution was cooled to room temperature and depressurized, and after termination of stirring, the liquid phase thereof was separated therefrom. Further, the solid reaction product was washed with a heptane solution of triisobutyl aluminum (1.25 mol/liter) three times by decantation to thereby adjust a volume of the heptane solution to 400 milliliter. Then, 73 milliliter of norbornene that was subjected to activated alumina treatment, dehydration and deoxygenation treatment, was added to the resultant solution, and the polymerization reaction was conducted at 80°C under an ethylene pressure of 0.7 MPa for 90 minutes. After completion of the reaction, the reaction solution was depressurized to recover grafted polyethylene. As a result, it was confirmed that the amount of the thus recovered grafted polyethylene was 30.8 g.
- a 1.6 liter stainless steel pressure-tight autoclave was charged with 400 milliliter of dehydrated heptane and 0.5 millimol of triisobutyl aluminum, and the mixture was stirred at room temperature for 10 minutes. Then, a whole amount of the supported catalyst prepared in the above step (1) was added to the autoclave.
- the resultant mixture was prepolymerized at 25°C under a propylene pressure of 0.3 MPa for 30 minutes to activate the catalyst, and then subjected to depressurization and blowing with nitrogen to remove unreacted propylene therefrom. Then, 0.81 milliliter of a heptane solution containing 0.5 millimol of 1,9-decadiene was added to the obtained reaction solution, and then hydrogen was introduced thereinto until reaching a hydrogen pressure of 0.02 MPa. After setting the reaction temperature at 60°C and introducing propylene until reaching a propylene partial pressure of 0.6 MPa, the polymerization reaction was initiated and continued for 30 minutes while controlling the reaction temperature to obtain polypropylene.
- the resultant reaction solution was cooled to room temperature and depressurized, and after termination of stirring, the liquid phase thereof was separated therefrom. Further, the obtained solid reaction product was washed with a heptane solution of triisobutyl aluminum (1.25 mol/liter) three times by decantation to thereby adjust a volume of the heptane solution to 400 milliliter. Then, 4.5 milliliter of a toluene solution containing [iPr(Cp)(Flu)ZrCl 2 ] in an amount of 5 micromole was dropped in the heptane solution, and the obtained solution was stirred at room temperature for 36 minutes.
- a 1.6 liter stainless steel pressure-tight autoclave was charged with 400 milliliter of dehydrated heptane and 0.5 millimol of triisobutyl aluminum, and the mixture was stirred at room temperature for 10 minutes. Then, the same supported catalyst as prepared in the above step (1) of Production Example 2 was added in an amount of 2 micromol in terms of zirconium atom to the autoclave.
- the resultant mixture was prepolymerized at 25°C under an ethylene pressure of 0.2 MPa for 30 minutes to activate the catalyst, and then subjected to depressurization and blowing with nitrogen to remove unreacted ethylene therefrom. Then, 0.81 milliliter of a heptane solution containing 0.5 millimol of 1,9-decadiene was added to the obtained reaction solution, and further hydrogen was introduced thereinto until reaching a hydrogen pressure of 0.05 MPa. After setting the reaction temperature at 60°C and introducing ethylene until reaching a ethylene partial pressure of 0.6 MPa, the polymerization reaction was initiated and continued for 45 minutes while controlling the reaction temperature to obtain polyethylene.
- the resultant reaction solution was cooled to room temperature, and depressurized and blown with nitrogen to remove unreacted ethylene. Further, the polymerization reaction was conducted at 60°C under a propylene pressure of 0.6 MPa for 180 minutes. After completion of the reaction, the reaction solution was depressurized to recover grafted polyethylene. As a result, it was confirmed that the yield of the thus recovered grafted polyethylene was 61.1 g.
- a 1.6 liter stainless steel pressure-tight autoclave was charged with 400 milliliter of dehydrated toluene and 0.5 milliliter of a toluene solution containing 0.2 millimol of 1,9-decadiene. Then, methyl aluminoxane (1.47 mol/liter; available from Albemarle Corporation; containing 14.5% by weight of trimethyl aluminum) was added to the autoclave such that the amount of methyl aluminoxane added was 4 millimol.
- the resultant mixture was stirred at room temperature for 10 minutes, and then 4 milliliter of a toluene solution containing [iPr(Cp)(Flu)ZrCl 2 ] and [rac-SiMe 2 (2-Me-4-Ph-Ind) 2 ZrCl 2 ] in amounts of 3 micromol and 1 micromol, respectively, was added thereto.
- the resultant mixture was graft-polymerized at 70°C under a propylene pressure of 0.3 MPa for 10 minutes. After completion of the reaction, the obtained reaction solution was cooled to room temperature and then depressurized to recover grafted polyethylene. As a result, it was confirmed that the yield of the thus recovered grafted polyethylene was 72.3 g.
- a 1.6 liter stainless steel pressure-tight autoclave was charged with 300 milliliter of dehydrated toluene, 0.3 millimol of p-3-butenyl styrene, 100 milliliter of styrene and 1 millimol of triisobutyl aluminum. Then, methyl aluminoxane (1.47 mol/liter; available from Albemarle Corporation; containing 14.5% by weight of trimethyl aluminum) was added to the autoclave such that the amount of methyl aluminoxane added was 4 millimol. The resultant mixture was stirred at room temperature for 10 minutes.
- the resultant mixture was prepolymerized at 25°C under a propylene pressure of 0.3 MPa for 30 minutes to activate the catalyst, and then subjected to depressurization and blowing with nitrogen to remove unreacted propylene therefrom. Then, 0.49 milliliter of a heptane solution containing 0.3 millimol of 1,9-decadiene was added to the obtained reaction solution, and further hydrogen was introduced thereinto until reaching a hydrogen pressure of 0.02 MPa. After setting the reaction temperature at 60°C and introducing propylene until reaching a propylene partial pressure of 0.6 MPa, the polymerization reaction was initiated and continued for 30 minutes while controlling the reaction temperature to obtain polypropylene.
- the resultant reaction solution was cooled to room temperature and depressurized, and after termination of the stirring, the liquid phase was separated therefrom. Further, the solid reaction product was washed with a heptane solution of triisobutyl aluminum (1.25 mol/liter) three times by decantation to thereby adjust a volume of the heptane solution to 100 milliliter.
- a 1.6 liter stainless steel pressure-tight autoclave was charged with 300 milliliter of dehydrated toluene, 0.3 millimol of p-3-butenyl styrene, 150 g of 1-octene, 100 milliliter of styrene and 1 millimol of triisobutyl aluminum. Then, methyl aluminoxane (1.47 mol/liter; available from Albemarle Corporation; containing 14.5% by weight of trimethyl aluminum) was added to the autoclave such that the amount of methyl aluminoxane added was 4 millimol. The resultant mixture was stirred at room temperature for 10 minutes.
- a 1.6 liter stainless steel pressure-tight autoclave was charged with 400 milliliter of dehydrated heptane, 0.3 millimol of 1,9-decadiene and 0.5 millimol of triisobutyl aluminum, and the resultant mixture was stirred at room temperature for 10 minutes.
- methyl aluminoxane (1.47 mol/liter; available from Albemarle Corporation; containing 14.5% by weight of trimethyl aluminum) was added to the autoclave such that the amount of methyl aluminoxane added was 2 millimol, and further 2 milliliter of a toluene solution containing as a metallocene catalyst, (Me 2 Si) 2 [3-CH 2 SiMe 3 -Ind] 2 ZrCl 2 and [rac-SiMe 2 (2-Me-4-Ph-Ind) 2 ZrCl 2 ] in amounts of 0.5 micromol and 1 micromol, respectively, was added to the above reaction mixture. After setting the reaction temperature at 50°C and introducing propylene until reaching a propylene partial pressure of 0.7 MPa, the polymerization reaction was initiated and continued for 30 minutes while controlling the reaction temperature to obtain polypropylene.
- the reaction solution was depressurized and blown with nitrogen to completely remove gaseous components such as unreacted propylene therefrom. After completion of the polymerization reaction, the obtained reaction solution was depressurized to recover polypropylene. As a result, it was confirmed that the yield of the thus recovered polypropylene was 62 g.
- EPDM-g-IPP was produced according to the method described in Example 1 of Japanese Patent Application Laid-open No. Hei3-28209. Various properties of the thus obtained EPDM-g-IPP are shown in Table 1.
- Amount of unreacted polyene represents a content of unreacted unsaturated groups in polyene present in the polymers to be copolymerized.
- Production Example 5 (Me 2 Si)Cp* (t-BuN)TiCl 2 4 0.3 70 30 96.7 rac-Me 2 Si[2-Me-4-Ph-Ind] 2 ZrCl 2 0.5
- Production Example 6 (Me 2 Si)CP (t-BuN)TiCl 2 4 0.7 50 30 55.7 iPr(Cp)(Flu)ZrCl 2 3
- the resin components shown in Table 3 were mixed and dissolved in 300 milliliter of p-xylene using 500 ppm of BHT as an antioxidant (based on the total amount of the resin components) under the conditions shown in Table 3. It was confirmed that the amount of the polymers dissolved was 3 to 3.3 g. After 3 hours, it was recognized that the resin components were uniformly dissolved. Then, the polymer mixed solution was charged into 3 liters of methanol while stirring to re-precipitate and recover solids. After filtering, the obtained solids were dried at 80°C under reduced pressure until reaching a constant weight, thereby obtaining the polyolefin composition.
- the resin composition produced in the above step (1) was formed into a plate shape using a heat press, and pulverized into pellets as a specimen.
- the specimen was subjected to solid 1 H-MMR by the above-mentioned method. The results are shown in Table 3.
- composition Measuring temperature (°C) Examples and Comparative Examples HDPE/ENB 100 Example 1; Example 2; Comparative Example 1; Comparative Example 2 IPP/ENB 130 Example 3; Example 4; Comparative Example 3 IPP/SPP 120 Example 5; Comparative Example 4 IPP/APP 30 Example 6; Example 7; Comparative Example 5 IPP/SPS 90 Example 8; Example 9; Comparative Example 6 IPP/HDPE 90 Example 10; Comparative Example 7
- the polyolefin-based resin compositions having specific properties were produced using the specific graft copolymers. For this reason, the miscibility between the polyolefins I and II as well as the interfacial adhesion therebetween can be sufficiently enhanced, and the particle size of dispersed particles can also be well controlled. As a result, the obtained resin compositions can be improved and well-controlled in properties such as mechanical strength, heat resistance, low-temperature impact strength and solvent resistance.
- the graft copolymers used in the respective Examples of the present invention have substantially no p-xylene insoluble components, and contains substantially no residual carbon-to-carbon double bonds. Therefore, the resin compositions of the respective Examples of the present invention which were produced using the graft copolymers, are free from blobs causing concentrated stress and can exhibit improved mechanical strength and excellent thermal stability.
- polyolefin-based resin composition that can be readily controlled in property-determining factors such as morphology and interfacial strength by combination of optional polyolefin-based resins, in particular, combination of non-compatible resins, and can provide a composite material composed of polyolefin-based resins which has excellent properties as required.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001030644 | 2001-02-07 | ||
JP2001030644 | 2001-02-07 | ||
PCT/JP2002/000952 WO2002062889A1 (fr) | 2001-02-07 | 2002-02-06 | Composition de resine polyolefinique |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1367093A1 true EP1367093A1 (fr) | 2003-12-03 |
EP1367093A4 EP1367093A4 (fr) | 2004-11-24 |
EP1367093B1 EP1367093B1 (fr) | 2005-12-14 |
Family
ID=18894833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP02711323A Expired - Lifetime EP1367093B1 (fr) | 2001-02-07 | 2002-02-06 | Composition de resine polyolefinique |
Country Status (5)
Country | Link |
---|---|
US (1) | US7193013B2 (fr) |
EP (1) | EP1367093B1 (fr) |
JP (1) | JP4237492B2 (fr) |
DE (1) | DE60207996T2 (fr) |
WO (1) | WO2002062889A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014052364A1 (fr) * | 2012-09-25 | 2014-04-03 | Chevron Phillips Chemical Company Lp | Systèmes catalytiques doubles de type métallocène et semi-sandwich pour la préparation de polymères à large distribution de poids moléculaires |
EP2891680A1 (fr) * | 2014-01-06 | 2015-07-08 | Borealis AG | Mélange de polymères avec ethylene-norbornene ou propylene-norbornene copolymer |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60207996T2 (de) * | 2001-02-07 | 2006-06-22 | Idemitsu Kosan Co. Ltd. | Polyolefinharzzusammensetzung |
FR2839976B1 (fr) * | 2002-05-21 | 2004-07-30 | Solvay | Composition polymere comportant un copolymere olefinique cyclique |
US7700707B2 (en) | 2002-10-15 | 2010-04-20 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions and articles made therefrom |
AU2003302033A1 (en) | 2002-10-15 | 2004-06-15 | Exxonmobil Chemical Patents Inc. | Multiple catalyst system for olefin polymerization and polymers produced therefrom |
US7482404B2 (en) * | 2004-02-17 | 2009-01-27 | The Goodyear Tire & Rubber Company | Liquid polymer |
US20090198031A1 (en) * | 2004-07-01 | 2009-08-06 | The Penn State Research Foundation | One-pot process and reagents for preparing long chain branched polymers |
US7713539B2 (en) * | 2004-07-19 | 2010-05-11 | Boston Scientific Scimed, Inc. | Medical devices containing radiation resistant block copolymer |
EP2891511A1 (fr) | 2013-11-22 | 2015-07-08 | Byk-Chemie GmbH | Polymère à base d'éthylène comme additif démoussant |
CN105017670B (zh) * | 2015-07-07 | 2018-04-20 | 四川塑金科技有限公司 | 一种聚苯乙烯管材的成型工艺 |
GB2565587A (en) * | 2017-08-18 | 2019-02-20 | Addivant Switzerland Gmbh | Insulation composition |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0490269A1 (fr) * | 1990-12-10 | 1992-06-17 | Idemitsu Kosan Company Limited | Copolymère greffé et son procédé de production |
EP0667359A1 (fr) * | 1992-10-28 | 1995-08-16 | Idemitsu Kosan Company Limited | Copolymeres d'olefines et procede pour leur production |
WO2001007493A1 (fr) * | 1999-07-26 | 2001-02-01 | Idemitsu Petrochemical Co., Ltd. | Macromonomere olefinique ramifie, copolymere olefinique greffe, et composition d'une resine olefinique |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0366411A3 (fr) * | 1988-10-28 | 1991-04-24 | Exxon Chemical Patents Inc. | Polymères d'éthylène-propylène-diène greffés par du propylène, leur méthode de préparation et leur usage dans des compositions de polypropylène |
JPH04288355A (ja) * | 1991-03-15 | 1992-10-13 | Showa Denko Kk | プロピレン系シート材料 |
ATE153680T1 (de) * | 1992-03-03 | 1997-06-15 | Idemitsu Kosan Co | Pfropfcopolymer, verfahren zu seiner herstellung und harzzusammensetzung, worin es enthalten ist |
US5455300A (en) | 1994-07-29 | 1995-10-03 | Montell North America Inc. | Graft copolymer of propylene polymer material impact modified with a heterophasic olefin polymer material |
US5543458A (en) * | 1995-01-31 | 1996-08-06 | Shell Oil Company | Process for making graft block copolymers by growing anionic polymer chains from functionalized polyolefin backbones |
DE19709667A1 (de) * | 1997-03-11 | 1998-09-17 | Basf Ag | Kammpolymere via Metallocenkatalyse |
US5981643A (en) * | 1997-10-09 | 1999-11-09 | Exxon Chemical Patents, Inc. | Depression of the glass transition temperature of polyolefins containing cyclic monomers |
US6515059B1 (en) * | 1997-11-18 | 2003-02-04 | Bfs Diversified Products, Llc | Utilization of devulcanized EPDM membrane in the manufacture of EPDM membrane, flashing and roof accessories |
DE19829397A1 (de) * | 1998-07-01 | 2000-01-05 | Basf Ag | Verwendung mikrophasenseparierter Polymermischungen für die Herstellung von permeablen Membranen |
DE60207996T2 (de) * | 2001-02-07 | 2006-06-22 | Idemitsu Kosan Co. Ltd. | Polyolefinharzzusammensetzung |
-
2002
- 2002-02-06 DE DE60207996T patent/DE60207996T2/de not_active Expired - Lifetime
- 2002-02-06 EP EP02711323A patent/EP1367093B1/fr not_active Expired - Lifetime
- 2002-02-06 WO PCT/JP2002/000952 patent/WO2002062889A1/fr active IP Right Grant
- 2002-02-06 US US10/467,298 patent/US7193013B2/en not_active Expired - Fee Related
- 2002-02-06 JP JP2002563235A patent/JP4237492B2/ja not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0490269A1 (fr) * | 1990-12-10 | 1992-06-17 | Idemitsu Kosan Company Limited | Copolymère greffé et son procédé de production |
EP0667359A1 (fr) * | 1992-10-28 | 1995-08-16 | Idemitsu Kosan Company Limited | Copolymeres d'olefines et procede pour leur production |
WO2001007493A1 (fr) * | 1999-07-26 | 2001-02-01 | Idemitsu Petrochemical Co., Ltd. | Macromonomere olefinique ramifie, copolymere olefinique greffe, et composition d'une resine olefinique |
Non-Patent Citations (1)
Title |
---|
See also references of WO02062889A1 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014052364A1 (fr) * | 2012-09-25 | 2014-04-03 | Chevron Phillips Chemical Company Lp | Systèmes catalytiques doubles de type métallocène et semi-sandwich pour la préparation de polymères à large distribution de poids moléculaires |
US8865846B2 (en) | 2012-09-25 | 2014-10-21 | Chevron Phillips Chemical Company Lp | Metallocene and half sandwich dual catalyst systems for producing broad molecular weight distribution polymers |
US9273159B2 (en) | 2012-09-25 | 2016-03-01 | Chevron Phillips Chemical Company Lp | Metallocene and half sandwich dual catalyst systems for producing broad molecular weight distribution polymers |
EP2891680A1 (fr) * | 2014-01-06 | 2015-07-08 | Borealis AG | Mélange de polymères avec ethylene-norbornene ou propylene-norbornene copolymer |
WO2015101667A1 (fr) * | 2014-01-06 | 2015-07-09 | Borealis Ag | Mélange de polymères : pehd comprenant un copolymère d'éthylène-norbornène ou un copolymère de propylène-norbornène |
Also Published As
Publication number | Publication date |
---|---|
EP1367093A4 (fr) | 2004-11-24 |
EP1367093B1 (fr) | 2005-12-14 |
DE60207996T2 (de) | 2006-06-22 |
WO2002062889A1 (fr) | 2002-08-15 |
JPWO2002062889A1 (ja) | 2004-06-10 |
JP4237492B2 (ja) | 2009-03-11 |
US7193013B2 (en) | 2007-03-20 |
DE60207996D1 (de) | 2006-01-19 |
US20040072950A1 (en) | 2004-04-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1408080B1 (fr) | Composition de resine a base de polyolefines | |
EP1367093B1 (fr) | Composition de resine polyolefinique | |
EP1241191B1 (fr) | Copolymere d'ethylene, composition de copolymere ethylene/alpha-olefine et composition de polymere de propylene contenant toutes deux le copolymere d'ethylene | |
JP4326802B2 (ja) | ポリオレフィン系樹脂組成物の製造方法 | |
KR20100044168A (ko) | 올레핀과 방향족 바이닐 화합물로 이루어지는 공중합체, 그의 제조 방법, 상기 공중합체를 포함하는 수지 조성물 및 상기 공중합체의 연신 성형품 | |
WO2017206043A1 (fr) | Mélanges de polyoléfine thermoplastique comprenant des composites séquencés comme agents de compatibilisation | |
JP2007084806A (ja) | プロピレン系樹脂組成物 | |
JP4068953B2 (ja) | プロピレン系樹脂組成物 | |
JP2023098910A (ja) | 低温用容器のための耐衝撃性改質組成物 | |
US20180051165A1 (en) | Composition for low temperature use containers | |
EP1917304B1 (fr) | Composition de résine à base de propylène | |
JP2004217896A (ja) | ポリプロピレン系樹脂組成物 | |
AU669503B2 (en) | Impact-resistant polyolefin molding composition | |
JP2002201321A (ja) | プロピレン重合体組成物および射出成形体 | |
JP5124262B2 (ja) | プロピレン系共重合体組成物 | |
JP2002348343A (ja) | オレフィン系重合体、その製造方法及び該重合体を含む熱可塑性樹脂組成物 | |
US11131130B2 (en) | Plastic living hinges with block composite polymer | |
JP2002348342A (ja) | スチレン系重合体、その製造方法及び該重合体を含む熱可塑性樹脂組成物 | |
JP3607427B2 (ja) | 熱可塑性エラストマー樹脂組成物 | |
JPH0948884A (ja) | ポリプロピレン組成物 | |
CA3068535A1 (fr) | Charnieres souples en plastique avec polymere composite sequence | |
JP2002348336A (ja) | オレフィン系重合体、その製造方法及び該重合体を含む熱可塑性樹脂組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20030806 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
A4 | Supplementary search report drawn up and despatched |
Effective date: 20041013 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: 7C 08L 45/00 B Ipc: 7C 08L 51/06 B Ipc: 7C 08L 51/00 B Ipc: 7C 08L 23/00 B Ipc: 7C 08L 25/00 B Ipc: 7C 08L 23/02 A |
|
17Q | First examination report despatched |
Effective date: 20041129 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: IDEMITSU KOSAN CO., LTD. |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE GB |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REF | Corresponds to: |
Ref document number: 60207996 Country of ref document: DE Date of ref document: 20060119 Kind code of ref document: P |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20060314 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20060915 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20060314 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20140129 Year of fee payment: 13 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 60207996 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20150901 |